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ZIRC
ZFIN ID: ZDB-PUB-120105-82
Ccm3 functions in a manner distinct from Ccm1 and Ccm2 in a zebrafish model of CCM vascular disease
Yoruk, B., Gillers, B.S., Chi, N.C., and Scott, I.C.
Date: 2012
Source: Developmental Biology 362(2): 121-131 (Journal)
Registered Authors: Chi, Neil C., Scott, Ian
Keywords: CCM3, cerebral cavernous malformations (CCMs), Stk25, vascular stability, angiogenesis, zebrafish
MeSH Terms:
  • Animals
  • Apoptosis Regulatory Proteins/genetics*
  • Apoptosis Regulatory Proteins/metabolism*
  • Central Nervous System Vascular Malformations/genetics*
  • Central Nervous System Vascular Malformations/pathology
  • Gene Knockdown Techniques
  • Heart Defects, Congenital/genetics*
  • Heart Defects, Congenital/pathology
  • In Situ Hybridization
  • Membrane Proteins/genetics*
  • Membrane Proteins/metabolism*
  • Microtubule-Associated Proteins/genetics
  • Microtubule-Associated Proteins/metabolism
  • Models, Biological
  • Morphogenesis/genetics*
  • Morpholinos/genetics
  • Mutation/genetics
  • Protein-Serine-Threonine Kinases/genetics
  • Protein-Serine-Threonine Kinases/metabolism
  • Proto-Oncogene Proteins/genetics*
  • Proto-Oncogene Proteins/metabolism*
  • Zebrafish
  • Zebrafish Proteins/genetics*
  • Zebrafish Proteins/metabolism*
PubMed: 22182521 Full text @ Dev. Biol.
FIGURES
ABSTRACT
Cerebral cavernous malformations (CCMs) are vascular anomalies of the central nervous system that arise due to mutations in genes encoding three unrelated proteins: CCM1 (KRIT1); CCM2 (Malcavernin/OSM) and CCM3 (PDCD10). Both biochemical and mutant studies suggest that CCM1 and CCM2 act as part of a physical complex to regulate vascular morphogenesis and integrity. In contrast, mouse Ccm3 mutant and in vitro cell culture data suggests an independent role for Ccm3. In this study, we sought to use the zebrafish model system to examine for the first time the role of ccm3 in cranial vessel development. We report that inhibition of zebrafish ccm3a/b causes heart and circulation defects distinct from those seen in ccm1 (santa) and ccm2 (valentine) mutants, and leads to a striking dilation and mispatterning of cranial vessels reminiscent of the human disease pathology. ccm3, but not ccm2, defects can be rescued upon overexpression of stk25b, a GCKIII kinase previously shown to interact with CCM3. Morpholino knockdown of the GCKIII gene stk25b results in heart and vasculature defects similar to those seen in ccm3 morphants. Finally, additional loss of ccm3 in ccm2 mutants leads to a synergistic increase in cranial vessel dilation. These results support a model in which CCM3 plays a role distinct from CCM1/2 in CCM pathogenesis, and acts via GCKIII activity to regulate cranial vasculature integrity and development. CCM3/GCKIII activity provides a novel therapeutic target for CCMs, as well as for the modulation of vascular permeability.
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